These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
241 related items for PubMed ID: 9334316
1. Translational repressor bruno plays multiple roles in development and is widely conserved. Webster PJ, Liang L, Berg CA, Lasko P, Macdonald PM. Genes Dev; 1997 Oct 01; 11(19):2510-21. PubMed ID: 9334316 [Abstract] [Full Text] [Related]
2. Drosophila cup is an eIF4E binding protein that associates with Bruno and regulates oskar mRNA translation in oogenesis. Nakamura A, Sato K, Hanyu-Nakamura K. Dev Cell; 2004 Jan 01; 6(1):69-78. PubMed ID: 14723848 [Abstract] [Full Text] [Related]
3. Region-specific activation of oskar mRNA translation by inhibition of Bruno-mediated repression. Kim G, Pai CI, Sato K, Person MD, Nakamura A, Macdonald PM. PLoS Genet; 2015 Jan 01; 11(2):e1004992. PubMed ID: 25723530 [Abstract] [Full Text] [Related]
4. oskar RNA plays multiple noncoding roles to support oogenesis and maintain integrity of the germline/soma distinction. Kanke M, Jambor H, Reich J, Marches B, Gstir R, Ryu YH, Ephrussi A, Macdonald PM. RNA; 2015 Jun 01; 21(6):1096-109. PubMed ID: 25862242 [Abstract] [Full Text] [Related]
9. Apontic binds the translational repressor Bruno and is implicated in regulation of oskar mRNA translation. Lie YS, Macdonald PM. Development; 1999 Mar 01; 126(6):1129-38. PubMed ID: 10021333 [Abstract] [Full Text] [Related]
10. Bruno negatively regulates germ cell-less expression in a BRE-independent manner. Moore J, Han H, Lasko P. Mech Dev; 2009 Jul 01; 126(7):503-16. PubMed ID: 19393317 [Abstract] [Full Text] [Related]
11. Oocyte polarity depends on regulation of gurken by Vasa. Tomancak P, Guichet A, Zavorszky P, Ephrussi A. Development; 1998 May 01; 125(9):1723-32. PubMed ID: 9521910 [Abstract] [Full Text] [Related]
13. The Drosophila Bruno paralogue Bru-3 specifically binds the EDEN translational repression element. Delaunay J, Le Mée G, Ezzeddine N, Labesse G, Terzian C, Capri M, Aït-Ahmed O. Nucleic Acids Res; 2004 May 01; 32(10):3070-82. PubMed ID: 15181172 [Abstract] [Full Text] [Related]
16. Patterning of the Drosophila oocyte by a sequential translation repression program involving the d4EHP and Belle translational repressors. Yarunin A, Harris RE, Ashe MP, Ashe HL. RNA Biol; 2011 May 01; 8(5):904-12. PubMed ID: 21788736 [Abstract] [Full Text] [Related]
17. Squid is required for efficient posterior localization of oskar mRNA during Drosophila oogenesis. Norvell A, Debec A, Finch D, Gibson L, Thoma B. Dev Genes Evol; 2005 Jul 01; 215(7):340-9. PubMed ID: 15791421 [Abstract] [Full Text] [Related]
18. A conserved 90 nucleotide element mediates translational repression of nanos RNA. Gavis ER, Lunsford L, Bergsten SE, Lehmann R. Development; 1996 Sep 01; 122(9):2791-800. PubMed ID: 8787753 [Abstract] [Full Text] [Related]
19. Control of oskar mRNA translation by Bruno in a novel cell-free system from Drosophila ovaries. Castagnetti S, Hentze MW, Ephrussi A, Gebauer F. Development; 2000 Mar 01; 127(5):1063-8. PubMed ID: 10662645 [Abstract] [Full Text] [Related]
20. Distinct roles of two conserved Staufen domains in oskar mRNA localization and translation. Micklem DR, Adams J, Grünert S, St Johnston D. EMBO J; 2000 Mar 15; 19(6):1366-77. PubMed ID: 10716936 [Abstract] [Full Text] [Related] Page: [Next] [New Search]